EHHADH

enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase
Identifiers
SymbolEHHADH
Alt. symbolsECHD
NCBI gene1962
HGNC3247
OMIM607037
Other data
EC number4.2.1.17
LocusChr. 3 q26.3-q28

EHHADH is a human gene that encodes for a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. Mutations of the gene are a cause of peroxisomal disorders such as Zellweger syndrome. [1]

See also

References

  1. ^ "EHHADH enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase [ Homo sapiens (human) ]". NCBI. 6 September 2017. Retrieved 12 September 2017.
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